Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
01379
CAS Number:
3262-72-4
Boc-L-serine
Purity:
≥ 99.5% (Chiral HPLC)
Synonym(s):
Boc-L-Ser-OH, Boc-L-β-Hydroxyalanine, (S)-Boc-2-amino-3-hydroxypropionic acid
Documents
$18.50 /5G
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-L-serine is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butyloxycarbonyl (Boc) protecting group, which enhances its stability and solubility, making it an ideal choice for the synthesis of complex peptides. Its unique structure allows for selective deprotection under mild conditions, facilitating the incorporation of serine into peptides without compromising the integrity of sensitive functional groups. Researchers often leverage Boc-L-serine in the development of therapeutic peptides, particularly in the fields of drug discovery and biotechnology, where precise amino acid sequences are crucial for biological activity.

In addition to its applications in peptide synthesis, Boc-L-serine serves as a valuable building block in the production of various bioactive compounds. Its hydroxyl group contributes to the formation of hydrogen bonds, enhancing the stability and activity of the resulting peptides. This compound is particularly advantageous for researchers focused on creating peptide-based drugs with improved efficacy and reduced side effects. With its favorable properties and broad applicability, Boc-L-serine stands out as an essential tool for professionals in the pharmaceutical and biotechnology industries.

Synonyms
Boc-L-Ser-OH, Boc-L-β-Hydroxyalanine, (S)-Boc-2-amino-3-hydroxypropionic acid
CAS Number
3262-72-4
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C8H15NO5
Molecular Weight
205.22
MDL Number
MFCD00037243
PubChem ID
294907
Melting Point
90 - 94 °C
Appearance
White powder
Optical Rotation
[a]D20 = -8.5 ± 2 º (C=3 in H2O)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-Ser-OH, Boc-L-β-Hydroxyalanine, (S)-Boc-2-amino-3-hydroxypropionic acid
CAS Number
3262-72-4
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C8H15NO5
Molecular Weight
205.22
MDL Number
MFCD00037243
PubChem ID
294907
Melting Point
90 - 94 °C
Appearance
White powder
Optical Rotation
[a]D20 = -8.5 ± 2 º (C=3 in H2O)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-L-serine is widely utilized in research focused on:

  • Peptide Synthesis: It serves as a protected amino acid in the synthesis of peptides, allowing for the selective introduction of serine residues without unwanted reactions.
  • Drug Development: Researchers use Boc-L-serine to create biologically active compounds, particularly in the development of pharmaceuticals targeting neurological disorders.
  • Bioconjugation: This compound is valuable in bioconjugation techniques, where it helps in attaching biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Protein Engineering: In protein engineering, Boc-L-serine is used to modify protein structures, improving their stability and functionality for various applications in biotechnology.
  • Research in Enzyme Activity: It plays a role in studying enzyme mechanisms, particularly those involving serine residues, providing insights into metabolic pathways and enzyme functions.

Citations